The DAnish VIdeo IntubaTION (DA-VITION) Study

Last updated: September 17, 2024
Sponsor: Lise Aunsholt
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

Video-directed endotracheal intubation

Clinical Study ID

NCT05884645
The DA-VITION study
  • All Genders

Study Summary

This study aims to train an AI for video-directed endotracheal intubation (VITION) to recognise the anatomical structures of the upper airway during video-directed endotracheal intubations.

Eligibility Criteria

Inclusion

Patients are eligible if they adhere to all the following inclusion criteria:

● Undergoing video-directed oral or nasal endotracheal intubation.

Exclusion criteria

Exclusion

Patients are excluded if they adhere to one of the exclusion criteria:

  • Upper airway malformations (e.g., laryngomalacia, vocal cord paralysis, andsubglottic stenosis).

  • Failed attempt by video laryngoscopy due to malfunctioning equipment.

  • Missing or corrupted video recording.

  • Informed consent is not obtained from the participants or participants' parents /legal guardians.

Study Design

Total Participants: 10000
Treatment Group(s): 1
Primary Treatment: Video-directed endotracheal intubation
Phase:
Study Start date:
May 01, 2023
Estimated Completion Date:
March 31, 2026

Study Description

Study design

The VITION study protocol describes the design of a prospective, observational study. Inclusion will commence in 2023 at the anesthesia and intensive care departments in the Capital Region of Denmark.

Participants

Patients across all ages are eligible for inclusion if they are undergoing video-directed oral or nasal endotracheal intubation.

Exclusion criteria

Patients are excluded if they adhere to one of the exclusion criteria:

  • Upper airway malformations (e.g., laryngomalacia, vocal cord paralysis, and subglottic stenosis17,18).

  • Failed attempt by video laryngoscopy due to malfunctioning equipment.

  • Missing or corrupted video recording.

  • Informed consent is not obtained from the participants or participants' parents / legal guardians.

Interventions and comparisons

This prospective, observational study will have no interventions or comparisons.

Primary objective

The primary objective is to characterize anatomical landmarks and performances of intubations in a large and diverse pool of clinicians and patients.

Connect with a study center

  • Capital Region of Denmark

    København,
    Denmark

    Active - Recruiting

  • Department of Neonatal and Pediatric Intensive Care, Blegdamsvej 9

    København, 2100
    Denmark

    Site Not Available

  • Rigshospitalet

    København, 2100
    Denmark

    Site Not Available

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